A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624458



Internal ID15501308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:162162540..162165966hg38UCSC Ensembl
Outerchr6:162583572..162586998hg19UCSC Ensembl
Outerchr6:162503562..162506988hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg383427
hg193427
hg183427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511921
Supporting Variants
Samples1
Known GenesPARK2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624458
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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